Hydrochloric Acid → HCID 68607770, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:13]=[C:12]([S:14](Cl)(=[O:16])=[O:15])[CH:11]=[C:6]([C:7]([O:9]C)=[O:8])[CH:5]=1.[CH3:19][NH:20][CH3:21].[OH-].[Na+].Cl>C1COCC1.C(OCC)(=O)C.CO>[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:13]=[C:12]([S:14](=[O:16])(=[O:15])[N:20]([CH3:21])[CH3:19])[CH:11]=[C:6]([C:7]([OH:9])=[O:8])[CH:5]=1Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
Dissolve commercially available 5-chlorosulfonyl-isophthalic acid dimethyl ester (422 mg, 1.43 mmol) in THF (10 mL) and add dimethylamine (2.0 M in THF, 2.5 mL, 5 mmol). Stir at room temperature 3 h, dilute with ethyl acetate, wash with 10% aqueous potassium carbonate, 0.1 N citric acid and saturated aqueous sodium chloride. Dry (magnesium sulfate), filter and concentrate. Dissolve the residue in acetone (10 mL) and methanol (5 mL). Add a solution of NaOH (60 mg, 1.43 mmol) in methanol (0.7 mL). Stir at room temperature 16 h and acidify with 1 N HCl to about pH=1. Partition between ethyl acetate and water, dry (magnesium sulfate) and concentrate to give the title compound.
Workup
- washwash with 10% aqueous potassium carbonate, 0.1 N citric acid and saturated aqueous sodium chloride
- dry with materialDry (magnesium sulfate)
- filtrationfilter
- concentrationconcentrate
- dissolutionDissolve the residue in acetone (10 mL)
- stirringStir at room temperature 16 h
- customPartition between ethyl acetate and water
- dry with materialdry (magnesium sulfate)
- concentrationconcentrate
Sources & evidence
- ORD record
- ord-d185c0662af6418eb20d9fc77049ceaf
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07585885B2
Reaction notes
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